Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H8O10S2 |
Molecular Weight | 352.295 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=CC(=O)OC2=C1C=C(OS(O)(=O)=O)C(OS(O)(=O)=O)=C2
InChI
InChIKey=SZNQDPUZKFSCNG-UHFFFAOYSA-N
InChI=1S/C10H8O10S2/c1-5-2-10(11)18-7-4-9(20-22(15,16)17)8(3-6(5)7)19-21(12,13)14/h2-4H,1H3,(H,12,13,14)(H,15,16,17)
Molecular Formula | C10H8O10S2 |
Molecular Weight | 352.295 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Sulmarin is a water-soluble coumarin derivative with vitamin P activity. In preclinical models Sulmarin facilitates excitatory transmission from parasympathetic fibers to the gastric musculature, increasing acetylcholine release. Sulmarin reduced the tone of isolated calf coronary arteries and also inhibited the contractile response of the arteries to angiotensin II amide (Hypertensin).
Originator
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 17:19:40 GMT 2023
by
admin
on
Sat Dec 16 17:19:40 GMT 2023
|
Record UNII |
73W96524XT
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Official Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Brand Name | English | ||
|
Common Name | English |
Classification Tree | Code System | Code | ||
---|---|---|---|---|
|
NCI_THESAURUS |
C45597
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
m10384
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | Merck Index | ||
|
CHEMBL2104898
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
SUB10747MIG
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
3703
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
13963
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
100000082952
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
3573
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
C74242
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
249-567-8
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
73W96524XT
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
DTXSID10183570
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY | |||
|
29334-07-4
Created by
admin on Sat Dec 16 17:19:40 GMT 2023 , Edited by admin on Sat Dec 16 17:19:40 GMT 2023
|
PRIMARY |
Related Record | Type | Details | ||
---|---|---|---|---|
|
SALT/SOLVATE -> PARENT |
Related Record | Type | Details | ||
---|---|---|---|---|
|
ACTIVE MOIETY |